| NDC Code | 68180-604-02 |
|---|
| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68180-604-02) |
|---|
| Product NDC | 68180-604 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Desvenlafaxine Succinate |
|---|
| Non-Proprietary Name | Desvenlafaxine Succinate |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20220825 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA204172 |
|---|
| Manufacturer | Lupin Pharmaceuticals, Inc. |
|---|
| Substance Name | DESVENLAFAXINE SUCCINATE |
|---|
| Strength | 25 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Cytochrome P450 2D6 Inhibitors [MoA], Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC] |
|---|